Genetic syndromes associated with deletions at chromosome 22q11 generally have been diagnosed during childhood based on a constellation of physical features. To investigate a reported association of velocardiofacial syndrome with psychotic disorders in adults, we assessed subjects with DSM-IV schizo
Generalized skeletal dysplasia in mother and daughter with 22q11 deletion syndrome
โ Scribed by Adachi, Masanori ;Tachibana, Katsuhiko ;Asakura, Yumi ;Nishimura, Gen ;Fukushima, Yoshimitsu ;Sakazume, Satoru
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 149 KB
- Volume
- 117A
- Category
- Article
- ISSN
- 0148-7299
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๐ SIMILAR VOLUMES
Skeletal anomalies in patients with a 22q11.2 deletion are reported infrequently. We report the skeletal findings in 108 patients with a 22q11.2 deletion, of whom 37 (36%) had a skeletal anomaly. Twenty-two patients (20%) had anomalies of the limbs, 7 of the upper limb, including preaxial or postaxi
The authors report that in the caption to Figure 1, the fourth sentence should have read ''The trigon of the right lateral ventricle is enlarged.'' The authors regret the error.